 Hypoprothrombinemias
"Hypoprothrombinemias" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Absence or reduced levels of PROTHROMBIN in the blood.
| Descriptor ID |
D007020
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| MeSH Number(s) |
C15.378.100.100.550 C15.378.100.141.550 C15.378.463.550 C16.320.099.550
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| Concept/Terms |
Hypoprothrombinemias- Hypoprothrombinemias
- Prothrombin Deficiency
- Deficiencies, Prothrombin
- Deficiency, Prothrombin
- Prothrombin Deficiencies
- Hypoprothrombinemia
- Deficiency, Factor II
- Deficiencies, Factor II
- Factor II Deficiencies
- Factor II Deficiency
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Below are MeSH descriptors whose meaning is more general than "Hypoprothrombinemias".
Below are MeSH descriptors whose meaning is more specific than "Hypoprothrombinemias".
This graph shows the total number of publications written about "Hypoprothrombinemias" by people in this website by year, and whether "Hypoprothrombinemias" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hypoprothrombinemias" by people in Profiles.
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Lefkowitz JB, Weller A, Nuss R, Santiago-Borrero PJ, Brown DL, Ortiz IR. A common mutation, Arg457-->Gln, links prothrombin deficiencies in the Puerto Rican population. J Thromb Haemost. 2003 Nov; 1(11):2381-8.
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Watzke HH, Lechner K, Roberts HR, Reddy SV, Welsch DJ, Friedman P, Mahr G, Jagadeeswaran P, Monroe DM, High KA. Molecular defect (Gla+14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X "Vorarlberg"). J Biol Chem. 1990 Jul 15; 265(20):11982-9.
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Johnson CA, Chung KS, McGrath KM, Bean PE, Roberts HR. Characterization of a variant prothrombin in a patient congenitally deficient in factors II, VII, IX and X. Br J Haematol. 1980 Mar; 44(3):461-9.
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